| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:55324473-55324565 | Common:1; Rare:19 | ||||
| chr16:55324583-55324802 | Rare:53 | ||||
| chr16:56540310-56540573 | Common:1; Rare:52 | ||||
| chr16:56610205-56610272 | Rare:17 | ||||
| chr16:56610303-56610531 | Common:1; Rare:46 | ||||
| chr16:56617357-56617582 | Common:4; Rare:47 | ||||
| chr16:56639433-56639749 | Common:4; Rare:51 | ||||
| chr16:56643224-56643734 | Common:7; Rare:109 | ||||
| chr16:56683552-56683869 | Common:7; Rare:54 | ||||
| chr16:66541933-66541977 | Common:1; Rare:15; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:68283814-68283894 | Rare:13 | ||||
| chr16:69324053-69324210 | Common:2; Rare:34 | ||||
| chr16:69718168-69718395 | Rare:60 | ||||
| chr16:70065772-70066142 | Common:2; Rare:113 | ||||
| chr16:72072976-72073249 | Common:1; Rare:50 |